AI Article Synopsis

  • Researchers created a 3-D model of human adipose tissue (AT) that mimics the natural structure found in the body, addressing issues with standard culture methods.
  • The model consists of spheroids made from human adipose progenitors, featuring organized endothelial networks that support mature adipocytes with lipid vacuoles.
  • When these spheroids were transplanted into immune-deficient mice, they successfully integrated with the mice's circulatory system, maintaining human adipocytes, indicating the model's potential for studying human AT.

Article Abstract

Native human subcutaneous adipose tissue (AT) is well organized into unilocular adipocytes interspersed within dense vascularization. This structure is completely lost under standard culture conditions and may impair the comparison with native tissue. Here, we developed a 3-D model of human white AT reminiscent of the cellular architecture found in vivo. Starting with adipose progenitors derived from the stromal-vascular fraction of human subcutaneous white AT, we generated spheroids in which endogenous endothelial cells self-assembled to form highly organized endothelial networks among stromal cells. Using an optimized adipogenic differentiation medium to preserve endothelial cells, we obtained densely vascularized spheroids containing mature adipocytes with unilocular lipid vacuoles. In vivo study showed that when differentiated spheroids were transplanted in immune-deficient mice, endothelial cells within the spheroids connected to the recipient circulatory system, forming chimeric vessels. In addition, adipocytes of human origin were still observed in transplanted mice. We therefore have developed an in vitro model of vascularized human AT-like organoids that constitute an excellent tool and model for any study of human AT.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6510792PMC
http://dx.doi.org/10.1038/s41598-019-43624-6DOI Listing

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